# FDA Inspection 1093677 - NeuroSync, Inc. - June 20, 2019

Source: https://www.keypedia.com/records/fda_inspections/neurosync-inc/73c05da3-0e1a-473c-aa3c-cee6086d9776
Source feed: FDA_Inspections

> FDA Inspection 1093677 for NeuroSync, Inc. on June 20, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1093677
- Company Name: NeuroSync, Inc.
- Inspection Date: 2019-06-20
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/neurosync-inc/e2eeae43-a0cd-41b7-b6bf-7e4e86628202

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7